Molekylärgenetisk analys av dilaterad cardiomyopati hos hund

Canine dilated cardiomyopathy (DCM) is a disease with high morbidity and mortality and with a high prevalence in certain breeds. Predominatly large breeds are affected, such as Great danes, Newfoundlands, Deerhounds and Dobermanns. One exception is Cocker spaniels, where both American and English Co...

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Main Author: Kanold, Anja
Format: L3
Language:Swedish
Inglés
Published: SLU/Dept. of Animal Breeding and Genetics (until 231231) 2007
Subjects:
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author Kanold, Anja
author_browse Kanold, Anja
author_facet Kanold, Anja
author_sort Kanold, Anja
collection Epsilon Archive for Student Projects
description Canine dilated cardiomyopathy (DCM) is a disease with high morbidity and mortality and with a high prevalence in certain breeds. Predominatly large breeds are affected, such as Great danes, Newfoundlands, Deerhounds and Dobermanns. One exception is Cocker spaniels, where both American and English Cocker spaniels are affected in a quite high frequency. Cardiomyopathy is characterised as a disease that affects the myocardium and gives an impaired heart function. To diagnose DCM following criteria have to be observed: 1. Dilation of the left ventricle. 2. Reduced systolic heart function. 3. Increased sphericity of the left ventricle. To be certain of the diagnosis, alternative reasons for the symptoms such as lung- and heart diseases with other etiologies have to be excluded Two different types of DCM have been found upon histological examination. One type where the myocytes are thinner than normal and have a wavy appearance – attenuated wavy fibers. There has also been observed a space between the myocytes which indicates edematous fluid. The alternative histological findings are infiltrates of fatty- and connective tissue. Since this is a disease of great suffering both for the dog and for its owner it would be of great interest to find the altered genes that gives an increased risk to develop this disease. Our study was done in a family of Newfoundlands where certain individuals were diagnosed with DCM of the wavy fibers type. Blood samples from dogs representing a few generations were available to us. We started our study with a candidate gene approach, and the gene of our choice was desmin, since it has been documented to be the cause of DCM in certain studies of human families. The histological appearance also indicated that a protein in the cytoskeleton is involved in the disease. The desmin gene was analysed in a few individuals by Polymerase Chain Reaction (PCR) and nucleotide sequencing of exon 8 in the desmin gene. When analysing our results we found a Single Nucleotide Polymorphism (SNP). The SNP was evaluated for genetic association to DCM. However, the SNP did not cause any change in amino acids and neither of the alleles showed association with DCM. The identified SNP can be used in future association mapping studies in a larger Newfoundland population to conclusively exclude desmin as a disease gene for DCM.
format L3
id RepoSLU11129
institution Swedish University of Agricultural Sciences
language swe
Inglés
publishDate 2007
publishDateSort 2007
publisher SLU/Dept. of Animal Breeding and Genetics (until 231231)
publisherStr SLU/Dept. of Animal Breeding and Genetics (until 231231)
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spelling RepoSLU111292017-09-28T07:50:51Z Molekylärgenetisk analys av dilaterad cardiomyopati hos hund Kanold, Anja DCM desmin kandidatgen genetisk predisposition SNP microsatelliter autosomal dominant nedärvning Canine dilated cardiomyopathy (DCM) is a disease with high morbidity and mortality and with a high prevalence in certain breeds. Predominatly large breeds are affected, such as Great danes, Newfoundlands, Deerhounds and Dobermanns. One exception is Cocker spaniels, where both American and English Cocker spaniels are affected in a quite high frequency. Cardiomyopathy is characterised as a disease that affects the myocardium and gives an impaired heart function. To diagnose DCM following criteria have to be observed: 1. Dilation of the left ventricle. 2. Reduced systolic heart function. 3. Increased sphericity of the left ventricle. To be certain of the diagnosis, alternative reasons for the symptoms such as lung- and heart diseases with other etiologies have to be excluded Two different types of DCM have been found upon histological examination. One type where the myocytes are thinner than normal and have a wavy appearance – attenuated wavy fibers. There has also been observed a space between the myocytes which indicates edematous fluid. The alternative histological findings are infiltrates of fatty- and connective tissue. Since this is a disease of great suffering both for the dog and for its owner it would be of great interest to find the altered genes that gives an increased risk to develop this disease. Our study was done in a family of Newfoundlands where certain individuals were diagnosed with DCM of the wavy fibers type. Blood samples from dogs representing a few generations were available to us. We started our study with a candidate gene approach, and the gene of our choice was desmin, since it has been documented to be the cause of DCM in certain studies of human families. The histological appearance also indicated that a protein in the cytoskeleton is involved in the disease. The desmin gene was analysed in a few individuals by Polymerase Chain Reaction (PCR) and nucleotide sequencing of exon 8 in the desmin gene. When analysing our results we found a Single Nucleotide Polymorphism (SNP). The SNP was evaluated for genetic association to DCM. However, the SNP did not cause any change in amino acids and neither of the alleles showed association with DCM. The identified SNP can be used in future association mapping studies in a larger Newfoundland population to conclusively exclude desmin as a disease gene for DCM. SLU/Dept. of Animal Breeding and Genetics (until 231231) 2007 L3 swe eng https://stud.epsilon.slu.se/11129/
spellingShingle DCM
desmin
kandidatgen
genetisk predisposition
SNP
microsatelliter
autosomal dominant nedärvning
Kanold, Anja
Molekylärgenetisk analys av dilaterad cardiomyopati hos hund
title Molekylärgenetisk analys av dilaterad cardiomyopati hos hund
title_full Molekylärgenetisk analys av dilaterad cardiomyopati hos hund
title_fullStr Molekylärgenetisk analys av dilaterad cardiomyopati hos hund
title_full_unstemmed Molekylärgenetisk analys av dilaterad cardiomyopati hos hund
title_short Molekylärgenetisk analys av dilaterad cardiomyopati hos hund
title_sort molekylärgenetisk analys av dilaterad cardiomyopati hos hund
topic DCM
desmin
kandidatgen
genetisk predisposition
SNP
microsatelliter
autosomal dominant nedärvning